NDC 0378-6201

Verapamil Hydrochloride PM

Verapamil Hydrochloride

Verapamil Hydrochloride PM is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Verapamil Hydrochloride.

Product ID0378-6201_18f8e1d8-fc82-43a2-b38e-f0d36c6e8383
NDC0378-6201
Product TypeHuman Prescription Drug
Proprietary NameVerapamil Hydrochloride PM
Generic NameVerapamil Hydrochloride
Dosage FormCapsule, Extended Release
Route of AdministrationORAL
Marketing Start Date2007-08-09
Marketing End Date2019-11-30
Marketing CategoryANDA / ANDA
Application NumberANDA078306
Labeler NameMylan Pharmaceuticals Inc.
Substance NameVERAPAMIL HYDROCHLORIDE
Active Ingredient Strength100 mg/1
Pharm ClassesP-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
NDC Exclude FlagN

Packaging

NDC 0378-6201-01

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0378-6201-01)
Marketing Start Date2007-08-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0378-6201-05 [00378620105]

Verapamil Hydrochloride PM CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078306
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-08-09
Marketing End Date2013-07-23

NDC 0378-6201-93 [00378620193]

Verapamil Hydrochloride PM CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078306
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-08-09
Marketing End Date2014-12-01

NDC 0378-6201-01 [00378620101]

Verapamil Hydrochloride PM CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078306
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-08-09
Marketing End Date2019-11-30

NDC 0378-6201-77 [00378620177]

Verapamil Hydrochloride PM CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA078306
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-08-09
Marketing End Date2017-11-28

Drug Details

Active Ingredients

IngredientStrength
VERAPAMIL HYDROCHLORIDE100 mg/1

OpenFDA Data

SPL SET ID:15f8fd1a-4a8e-4949-8c5c-dd7c897b0791
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 897590
  • 897584
  • 897596
    • UPC Code
  • 0303786203772

    • Pharmacological Class

    • P-Glycoprotein Inhibitors [MoA]
    • Calcium Channel Antagonists [MoA]
    • Calcium Channel Blocker [EPC]
    • Cytochrome P450 3A4 Inhibitors [MoA]
    • Cytochrome P450 3A Inhibitors [MoA]

    NDC Crossover Matching brand name "Verapamil Hydrochloride PM" or generic name "Verapamil Hydrochloride"

    NDCBrand NameGeneric Name
    0378-6202Verapamil Hydrochloride PMVerapamil Hydrochloride PM
    0378-6201Verapamil Hydrochloride PMVerapamil Hydrochloride PM
    0378-6203Verapamil Hydrochloride PMVerapamil Hydrochloride PM
    0025-1861CALANverapamil hydrochloride
    0025-1891CALAN SRverapamil hydrochloride
    0025-1901CALAN SRverapamil hydrochloride
    0025-1911CALAN SRverapamil hydrochloride
    0025-2712CALAN SRverapamil hydrochloride
    0025-2818CALAN SRverapamil hydrochloride
    0025-2924CALAN SRverapamil hydrochloride
    0093-3043Verapamil Hydrochlorideverapamil hydrochloride
    0093-3044Verapamil Hydrochlorideverapamil hydrochloride
    0093-3045Verapamil Hydrochlorideverapamil hydrochloride
    0378-0512Verapamil Hydrochlorideverapamil hydrochloride
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